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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2409036생성일: 2026년 10월 26일

Trimethylsilylacetylene → 5-Fluoro-2-((trimethylsilyl)ethynyl)pyridin-3-amine

https://huagongshe.com/reaction/2409036

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylsilylacetyleneHCID 66111—
반응물2-Bromo-5-fluoropyridin-3-amineHCID 40427367—
촉매HCID 178418476HCID 178418476—
용매TetrahydrofuranHCID 8028—
생성물5-Fluoro-2-((trimethylsilyl)ethynyl)pyridin-3-amineHCID 8668985155.5%

반응 단계

To a mixture of 2-bromo-5-fluoropyridin-3-amine (3.3 g, 17.3 mmol), TEA (7.3 mL, 51.9 mmol), PdCl2(PPh3)2 (1.2 g, 1.73 mmol), and Cu(I)I (0.33 g, 1.73 mmol) in THF (50 mL) at 0° C. under nitrogen was added a solution of (trimethylsilyl)acetylene (3.39 mL, 34.6 mmol). The mixture was stirred at RT for 2 h and then concentrated under reduced pressure. The residue was purified by SiO2 chromatography eluting with petroleum ether/EtOAc (5:1) to afford 2.0 g (915) of 5-fluoro-2-((trimethylsilyl)ethynyl)pyridin-3-amine as a yellow solid. MS (ESI): m/z=209.1 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08815877B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-4035b68c98084901a958e68b87aef528
출처 메모uspto-grants-2014_08